US1908712A - Process of making dibenzanthrone - Google Patents
Process of making dibenzanthrone Download PDFInfo
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- US1908712A US1908712A US322964A US32296428A US1908712A US 1908712 A US1908712 A US 1908712A US 322964 A US322964 A US 322964A US 32296428 A US32296428 A US 32296428A US 1908712 A US1908712 A US 1908712A
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- dibenzanthrone
- benzanthrone
- caustic
- fusion
- finely divided
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/22—Dibenzanthrones; Isodibenzanthrones
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- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented May 16, 1933 UNITED STATES PATENT OFFICE A LUCAS P. KYRIDES, F BUFFALO, NEW YORK, ASSIGNOR TO NATIONAL ANILINE &
CHEMICAL COMPANY, IN (2., OF NEW YORK, N. Y., A CORPORATION OF NEW YORK PROCESS OF MAKING DIBENZAN'I'HRONE This invention relates to improvements in the production of dibenzanthrone (Indanthrene dark blue BO, Colour Index #1Q99) by the fusion of benzanthrone With caustic alkali.
It has heretofore been proposed to produce dibenzanthrone by fusing 1 part benzanthrone with 6 parts caustic potash at a temperature of about 250 (1, with the addition of a sugar, such as glucose, to the fused caus- I tic before addition of the benzanthrone there to (E. P. 126,7 WVhen the fusion is carried out in this way, excessive foamingresults and the fusion mass becomes viscous and diflicult to stir toward the end of the reaction. a 7
It has also been proposed to carry out the fusion with 1 part benzanthro-ne, 1 part caustic potash and 4.2 parts of a high boiling mineral oil at a temperature of 215 230 C. with theaddition of an organic reducing agent, such as dextrine (U. S. Patent 1,583,258) As thus carried out, the removal ofthe last traces of the mineral oil is difiicult. It has also been proposed to carry out the fusion using from 1.5 to l parts caustic potash per part of benzanthroire, without the use of dextrine or other organic reducing ma terial, and in the presence of solvents such as monochlorbenzene, naphthalene, or an alcohol, but the recovery of the solvent introduces a disadvantage.
The products above obtained contain large amounts of a non-vatable substance having practically no tinctorial value, and a vatable portion comprising essentially dibenzanthrone, which has tinctorial properties. The non-vatable substance not only has little or no utility as a dyestuff, but is a diluent of the dyestuff and therefore is preferably re moved. The elimination of this non-vatable substance is accomplished (U. S. Patent 1,478,027) by treating the fusion mass with dilute caustic soda solution and hydrosulfite, whereby the dyestuif is reduced to its leuco form and goes into solution, while the insoluble non-vatable portion is filtered off. The filtrate is then blown with air to precipitate the dyestufl". 7
One of'the objects of this invention is to Application filed November 30, 1928. Serial No. 322,964.
hydrcsulfite subsequently needed for purify-- ing the dycstuif. These and other objects Will be readily apparent to those skilled in the art from a consideration of the disclosure in the specification and claims.
According to the present invention, it has been found that in the production of .dibenzanthrone the proportion of caustic potash to benzanthrone in the fusion can be considerably reduced Without materially increasing the viscosity of the melt, and without necessitating the use of a solvent, a diluent, or an organic reducing agent. The present invention particularly contemplates the fusion of 1 part benzanthrone with as little as about 2.5 parts caustic potash in the presence of a finely divided metal which is capable of reacting With caustic alkali to pro duce hydrogen, as a reducing agent. The resulting product contains the dibenzanthrone mostly, if not all, in the reduced or leuco state. I
The invention will be illustrated by the following example, but it will be understood that the invention is not limited thereto. The parts are by weight.
EwampZa-l parts caustic potash (about 86% KOI-Dis heated to about 220280 C. with constant agitation in a covered iron fusion kettle equipped with a propeller agitator, a feed line for the introduction of gases, and a manhole for the introduction of solid material. A current of ammonia gas is continuously passed through the fusion kettle to sweep out and exclude air. A mixture of 67 7 parts powdered benzanthrone (about 90% pure) and 4.4 parts aluminum powder or aluminum bronze is introduced into the fusion kettle through the manhole as fast as 1s possible without causing excessive foaming. When all of the mixture has been added, the
melt is heated at about 23524.0 C. for
about one hour longer, or until the reaction is completed. It is then treated with about 5000-6000 parts of water, and a sufficient 5 amount of hydrosulfite, if necessary, to reduce the dyestuff to the leuco condition, and the insoluble material is filtered oil. The filtrate is then blown with air to precipitate the dyestuff.
In the foregoing example, the molecular ratio of caustic potash to benzanthrone is about 11 to 1. Higher or lower molar proportions of caustic may be used, if desired, but the proportions given in the above example are those preferred. Part of the caustic potash may be replaced by caustic soda if desired. 7
'VVhile the function of the finely divided metal used in this process is not definitely known, it is believed that the metal has a reducing action in the fusion which is due to the nascent hydrogen produced; This theory is supported by the fact that the dibenzanthrone thus produced is mostly in its leuco form. By excluding air from the fusion, the color produced is preserved in its leuco form, so that less hydrosulfite is required subsequently to accomplish its solution for the purpose of purification.
The viscosity of the fusion mass is less than when an organic reducing agent is used in the fusion. Consequently, agitation can be carried out readily throughout the fusion, thus preventing local overheating and in 353 creased formation of by-products. The process does not entail'the recovery of solvents since none are used.
In place of the aluminum powder, an equivalent portion of finely divided zinc or other metal which is capable of reacting with caustic alkali to produce hydrogen may be used with almost equally good results. It is desirable that the metal used shall be finely divided so as to secure a quick reaction between the metal and the caustic.
Care should be taken to remove the air from the fusion-kettle, since otherwise it may form an explosive mixture with the hydrogen evolved. For this purpose, the air space in the fusion kettle is swept by a stream of ammonia gas or other inert gas which preserves. a non-oxidizing atmosphere in the fusion kettle. Exclusion of air from the fusion kettle is desirable also for the reason that oxidation of the leuco dyestulf during the fusion is prevented.
It is obvious that various changes may be made in the example given without departing from the spirit or scope of the invention as defined in the following claims.
I claim: I
1. In the production of dibenzanthrone,
the process which comprises fusing together. benzanthrone, caustic alkali, and a finely divided metal which is capable of reacting with caustic alkali to produce hydrogen.
2. In the production of dibenzanthrone, the process which comprises fusing together benzanthrone, caustic potash and finely divided aluminum.
3. In the production of dibenzanthrone, the improvement which comprises fusing together benzanthrone, caustic potash and a.
finely divided metal which is capable of reacting with caustic potash to produce hydrogen.
4. In the production of dibenzanthrone,
the process which comprises heating 185 parts caustic potash, 67 parts powdered benzanthrone and 4.4: parts finely divided aluminum at a temperature of-about 220250 C.
5. In the production of dibenzanthrone, the process which comprises heating benzanthrone, eaustic potash and a finely divided metal which is capable of reacting with caustic potash to produce hydrogen, at a temperature of 220-2 i0 (l.
6. In the production of dibenzanthrone, the process which comprises heating caustic potash to about 220230 (1, adding thereto in small portions a'mixture of benzanthrone with a finely divided metal which is capable of reacting with caustic pot-ash to produce hydrogen, and heating at about 2352 l0C. until reaction is complete. 3
7'. In." the production of dibenzanthrone, the process which comprises heating caustic potash to about 220230 0., adding thereto in small portions a mixture of benzanthrone with finely divided aluminum, and heating at about 2352 l0 C. until reaction is complete.
8. In the production of dibenzanthrone, the process which comprises fusing together about 67 parts benzanthrone, about 185 parts caustic potash and a finely divided metal which is capable ofreacting with caustic potash to produce hydrogen.
9. In the production of 'dibenzantln'one, the process which comprises fusing, together about 67 parts benzanthrone, about 185 parts caustic potash and finely divided aluminum.
10. In the production of dibenzanthrone, the process which comprisesfusing benzanthrone with about 2.5 times its Weight of caustic potash and with a finely divided metal which is capable of reacting with caustic potash to produce hydrogen. 1
11. In the production of dibenzanthrone, the improvement which comprises fusing caustic potash, adding benzanthrone and fine: 1y divided aluminum thereto, and fusing the resulting mixture.
12. In the production of dibenzanthrone, the process which. comprises heating, caustic alkali, a finely divided meta-lwhich is capable of reacting with caustic alkali to produce hydrogen, and benzanthrone ata reaction temperature.
13. In the production of dibenzanthrone, the process which comprises heating benzanthrone, caustic potash and finely divided aluminum at a reaction temperature.
14. In the production of dibenzanthrone, the process which comprises fusing together benzanthrone, causticalkali,and a finely divided metal which is capable of reacting with caustic alkali to produce hydrogen, while excluding air from the reaction mixture.
15. In the produotion'of dibenzanthrone, the process which comprises fusing together benzanthrone, caustic alkali, and a finely divided metal which is capable of reacting with caustic alkali to produce hydrogen, while maintaining an atmosphere of ammonia in contact with the reaction mixture.
16. In the production of dibenzanthrone, the improvement which comprises fusing together benzanthrone, caustic potash and a finely divided metal which is capable of reacting with caustic potash to produce hydrogen, while maintaining a non-oxidizing atmosphere in contact with the reaction mixture.
17. In the production of dibenzanthrone, the process which comprises fusing caustic potash at a temperature of 220 to 240 (3., adding thereto in small portions a mixture of benzanthrone and aluminum powder, fusing the resulting mixture, and excluding air by maintaining an atmosphere of ammonia in contact with the reaction mixture.
In testimony whereof I affix my signature.
LUCAS P. KYRIDES.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US322964A US1908712A (en) | 1928-11-30 | 1928-11-30 | Process of making dibenzanthrone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US322964A US1908712A (en) | 1928-11-30 | 1928-11-30 | Process of making dibenzanthrone |
Publications (1)
Publication Number | Publication Date |
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US1908712A true US1908712A (en) | 1933-05-16 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US322964A Expired - Lifetime US1908712A (en) | 1928-11-30 | 1928-11-30 | Process of making dibenzanthrone |
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US (1) | US1908712A (en) |
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1928
- 1928-11-30 US US322964A patent/US1908712A/en not_active Expired - Lifetime
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